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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04277520
Other study ID # ASFD-ENDO-1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2020
Est. completion date July 1, 2021

Study information

Verified date July 2021
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate postoperative pain after endodontic instrumentation using rotation, reciprocation and adaptive motion.


Description:

Post operative pain assessment is done at the end of the session Visual Analog Scale (VAS) questionnaires were handed out to the patients and they were asked to assign a number correlating to their post-treatment pain, with 0 representing no pain and 10 representing the most severe pain imaginable.These scores were marked in intervals of 6, 12, 24, 48 and 72 h following endodontic treatment.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date July 1, 2021
Est. primary completion date July 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: 1. Medically free patients with good health. 2. Patient's age between 18_50 3. Mandibular first molars teeth diagnosed clinically and radiographically as acute irreversible pulpitis with no evidence of apical pathosis 4. Positive patient's acceptance for participation in the study Exclusion Criteria: - Root resorption - Non restorable teeth. - Pregnancy. - Systematic disease as hypertension ,diabetes . - Psychologically disturbance. - Need for prophylactic antibiotics

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Root canal therapy
Different types of instrumentation motions during root canal therapy

Locations

Country Name City State
Egypt Faculty of Dentistry, Ainshams University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

Gambarini G, Testarelli L, De Luca M, Milana V, Plotino G, Grande NM, Rubini AG, Al Sudani D, Sannino G. The influence of three different instrumentation techniques on the incidence of postoperative pain after endodontic treatment. Ann Stomatol (Roma). 2013 Mar 20;4(1):152-5. doi: 10.11138/ads.0152. Print 2013 Jan. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary monitoring the change in postoperative pain following root canal treatment At the end of the session Visual Analog Scale (VAS) questionnaires were handed out to the patients and they were asked to assign a number correlating to their post-treatment pain, following endodontic treatment with 0 representing no pain and 10 representing the most severe pain 72 hours
Secondary 6-hour post operative pain assessment At the end of the session Visual Analog Scale (VAS) questionnaires were handed out to the patients and they were asked to assign a number correlating to their post-treatment pain after 6 hours, following endodontic treatment with 0 representing no pain and 10 representing the most severe pain 6 hours
Secondary 12-hour post operative pain assessment At the end of the session Visual Analog Scale (VAS) questionnaires were handed out to the patients and they were asked to assign a number correlating to their post-treatment pain after 12 hours, following endodontic treatment with 0 representing no pain and 10 representing the most severe pain 12 hours
Secondary 24-hour post operative pain assessment At the end of the session Visual Analog Scale (VAS) questionnaires were handed out to the patients and they were asked to assign a number correlating to their post-treatment pain after 24 hours, following endodontic treatment with 0 representing no pain and 10 representing the most severe pain 24 hours
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